FDA applicant

Sturgeon Engineering Co.

Petrolia, CA2 decisions1985–19850 recalls

FDA records 2 decisions for Sturgeon Engineering Co. (Petrolia, CA) in 1985: 2 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and EKK (Spreader, Pulp Canal Filling Material…). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Sturgeon Engineering Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sturgeon Engineering Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sturgeon Engineering Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Sturgeon Engineering Co.

Which product codes does it file in?

What has FDA decided for it lately?